Medline Industries, Inc. DYND74262Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10080196862924), received between May 28, 2026 and Sep 18, 2026 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (5 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 18, 2026Loss of or Failure to Bond

  It was reported that "When the dressing is pulled apart the sticky part is not coming off with the tab when you separate it."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50817288 ↗
• MalfunctionSep 15, 2026Loss of or Failure to Bond; Component Missing

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50778577 ↗
• MalfunctionSep 14, 2026Loss of or Failure to Bond

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50763517 ↗
• MalfunctionSep 14, 2026Loss of or Failure to Bond

  It was reported that "Issue component Adhesive1-EA-52280 DRSG SURESITE 2 3/8X2 3/4FRAME not sticking."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50753316 ↗
• MalfunctionMay 28, 2026Loss of or Failure to Bond

  IT WAS REPORTED THAT THE DRESSING DOES NOT STICK TO THE PATIENT AND CAUSES TO USE TAGDERM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25325081 ↗